"pinitol" meaning in All languages combined

{
  "forms": [
    {
      "form": "pinitols",
      "tags": [
        "plural"
      ]
    }
  ],
  "head_templates": [
    {
      "args": {
        "1": "~"
      },
      "expansion": "pinitol (countable and uncountable, plural pinitols)",
      "name": "en-noun"
    }
  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "senses": [
    {
      "categories": [
        {
          "kind": "other",
          "name": "English entries with incorrect language header",
          "parents": [
            "Entries with incorrect language header",
            "Entry maintenance"
          ],
          "source": "w"
        },
        {
          "kind": "topical",
          "langcode": "en",
          "name": "Organic compounds",
          "orig": "en:Organic compounds",
          "parents": [
            "Matter",
            "Chemistry",
            "Nature",
            "Sciences",
            "All topics",
            "Fundamental"
          ],
          "source": "w"
        }
      ],
      "derived": [
        {
          "word": "D-pinitol"
        }
      ],
      "examples": [
        {
          "ref": "2001, Ryszard J. Górecki, “5: Seed Physiology and Biochemistry”, in C. L. Hedley, editor, Carbohydrates in Grain Legume Seeds: Improving Nutritional Quality and Agronomic Characteristics, CABI Publishing, page 126",
          "text": "Galactosylononitol and galactosyl pinitol A could also substitute for galactinol in the synthesis of stachyose from raffinose (Peterbaur and Richter, 1998; Hoch et al, 1999; Fig. 5.2, equations 10 and 11).",
          "type": "quotation"
        },
        {
          "ref": "2007, Tomas Hudlicky, Josephine W. Reed, The Way of Synthesis: Evolution of Design and Methods for Natural Products, Wiley, page 149",
          "text": "The reader can once more appreciate the lack of suitable language to describe these design principles; the thought process that led to the enantiodivergent synthesis of pinitols was far less arduous than the attempts to verbalize it.",
          "type": "quotation"
        },
        {
          "ref": "2014, T. K. Lim, Edible Medicinal and Non Medicinal Plants, Volume 8: Flowers, Springer, page 492",
          "text": "The use of B. spectabilis leaves as an antidiabetic led to the isolation of its hypoglycaemic principle, pinitol, from the leaves (Narayanan et al. 1987). Pinitol was determined to be a methyl ester of chiro-inositol and elucidated as 3-O-methyl1,2,4-cis-3,5,6-trans-hexahydroxycyclohexanol.",
          "type": "quotation"
        }
      ],
      "glosses": [
        "A cyclitol with antidiabetic activity, first identified in the sugar pine (Pinus lambertiana)."
      ],
      "id": "en-pinitol-en-noun-y6hKYTLq",
      "links": [
        [
          "organic chemistry",
          "organic chemistry"
        ],
        [
          "cyclitol",
          "cyclitol"
        ],
        [
          "antidiabetic",
          "antidiabetic"
        ],
        [
          "sugar pine",
          "sugar pine"
        ]
      ],
      "raw_glosses": [
        "(organic chemistry) A cyclitol with antidiabetic activity, first identified in the sugar pine (Pinus lambertiana)."
      ],
      "related": [
        {
          "word": "D-pinitol dehydrogenase"
        }
      ],
      "tags": [
        "countable",
        "uncountable"
      ],
      "topics": [
        "chemistry",
        "natural-sciences",
        "organic-chemistry",
        "physical-sciences"
      ],
      "wikipedia": [
        "pinitol"
      ]
    }
  ],
  "word": "pinitol"
}

{
  "derived": [
    {
      "word": "D-pinitol"
    }
  ],
  "forms": [
    {
      "form": "pinitols",
      "tags": [
        "plural"
      ]
    }
  ],
  "head_templates": [
    {
      "args": {
        "1": "~"
      },
      "expansion": "pinitol (countable and uncountable, plural pinitols)",
      "name": "en-noun"
    }
  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "related": [
    {
      "word": "D-pinitol dehydrogenase"
    }
  ],
  "senses": [
    {
      "categories": [
        "English countable nouns",
        "English entries with incorrect language header",
        "English lemmas",
        "English nouns",
        "English terms with quotations",
        "English uncountable nouns",
        "Entries using missing taxonomic name (species)",
        "en:Organic compounds"
      ],
      "examples": [
        {
          "ref": "2001, Ryszard J. Górecki, “5: Seed Physiology and Biochemistry”, in C. L. Hedley, editor, Carbohydrates in Grain Legume Seeds: Improving Nutritional Quality and Agronomic Characteristics, CABI Publishing, page 126",
          "text": "Galactosylononitol and galactosyl pinitol A could also substitute for galactinol in the synthesis of stachyose from raffinose (Peterbaur and Richter, 1998; Hoch et al, 1999; Fig. 5.2, equations 10 and 11).",
          "type": "quotation"
        },
        {
          "ref": "2007, Tomas Hudlicky, Josephine W. Reed, The Way of Synthesis: Evolution of Design and Methods for Natural Products, Wiley, page 149",
          "text": "The reader can once more appreciate the lack of suitable language to describe these design principles; the thought process that led to the enantiodivergent synthesis of pinitols was far less arduous than the attempts to verbalize it.",
          "type": "quotation"
        },
        {
          "ref": "2014, T. K. Lim, Edible Medicinal and Non Medicinal Plants, Volume 8: Flowers, Springer, page 492",
          "text": "The use of B. spectabilis leaves as an antidiabetic led to the isolation of its hypoglycaemic principle, pinitol, from the leaves (Narayanan et al. 1987). Pinitol was determined to be a methyl ester of chiro-inositol and elucidated as 3-O-methyl1,2,4-cis-3,5,6-trans-hexahydroxycyclohexanol.",
          "type": "quotation"
        }
      ],
      "glosses": [
        "A cyclitol with antidiabetic activity, first identified in the sugar pine (Pinus lambertiana)."
      ],
      "links": [
        [
          "organic chemistry",
          "organic chemistry"
        ],
        [
          "cyclitol",
          "cyclitol"
        ],
        [
          "antidiabetic",
          "antidiabetic"
        ],
        [
          "sugar pine",
          "sugar pine"
        ]
      ],
      "raw_glosses": [
        "(organic chemistry) A cyclitol with antidiabetic activity, first identified in the sugar pine (Pinus lambertiana)."
      ],
      "tags": [
        "countable",
        "uncountable"
      ],
      "topics": [
        "chemistry",
        "natural-sciences",
        "organic-chemistry",
        "physical-sciences"
      ],
      "wikipedia": [
        "pinitol"
      ]
    }
  ],
  "word": "pinitol"
}